반응 #631988

ord-f2d9ff5b15cc40b9a9cb882f8559e4d9

반응 방정식

Cl
HCl
CC1=CCCC(C)(C)C1C(=O)CC(C)O
3-hydroxy-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1-butanone
CCN(CC)CC
NEt3
Cc1ccc(S(=O)(=O)Cl)cc1
tosylchloride
CC1=CCCC(C)(C)C1C(=O)CC(C)OS(=O)(=O)c1ccc(C)cc1
product
수율 50.0%
CC1=CCCC(C)(C)C1C(=O)CC(C)OS(=O)(=O)c1ccc(C)cc1
1-methyl-3-oxo-3-(2,6,6-trimethyl-2-cyclohexen-1-yl)propyl 4-methyl-benzenesulfonate
수율 50.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted twice with ether
  2. 2
    세척washed with water, saturated aqueous NaHCO3
  3. 3
    건조Finally, the organic phases were dried over Na2SO4
  4. 4
    농축concentrated at 50-60°/0.03 mbar)

실험 절차

To a solution of 3-hydroxy-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1-butanone (1.00 g, 92% pure, 4.38 mmol), DMAP (100 mg), and NEt3 (1.0 ml, 7.2 mmol) in CH2Cl2 (20 ml) was added, at 0° C., tosylchloride (2.02 g, 10.56 mmol). The reaction medium was stirred at room temperature for 4 days. Then, the mixture was acidified with concentrated HCl and extracted twice with ether and washed with water, saturated aqueous NaHCO3 and then with saturated aqueous NaCl. Finally, the organic phases were dried over Na2SO4, concentrated at 50-60°/0.03 mbar). 0.76 g of product were thus obtained (yield: 50%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07935669B2uspto-grants-2011_05